Chiral acetylenic sulfoxide in enantioselective synthesis of yohimbine alkaloid

Albert W.M. Lee; W. H. Chan; T. Mo

doi:10.1016/S0040-4039(97)00519-4

Chiral acetylenic sulfoxide in enantioselective synthesis of yohimbine alkaloid

Albert W.M. Lee^*
, W. H. Chan
, T. Mo

^*Corresponding author for this work

Department of Chemistry

Research output: Contribution to journal › Journal article › peer-review

17 Citations (Scopus)

Abstract

Through Michael addition/acid induced cyclization of secondary amine to chiral acetylenic sulfoxide followed by Pummerer cyclization, an approach to the enantioselective syntheses of pentacyclic yohimbine alkaloids is presented.

Original language	English
Pages (from-to)	3001-3004
Number of pages	4
Journal	Tetrahedron Letters
Volume	38
Issue number	17
DOIs	https://doi.org/10.1016/S0040-4039(97)00519-4
Publication status	Published - 28 Apr 1997

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@article{34414435e0434b39a9dbee28fcbe7712,

title = "Chiral acetylenic sulfoxide in enantioselective synthesis of yohimbine alkaloid",

abstract = "Through Michael addition/acid induced cyclization of secondary amine to chiral acetylenic sulfoxide followed by Pummerer cyclization, an approach to the enantioselective syntheses of pentacyclic yohimbine alkaloids is presented.",

author = "Lee, \{Albert W.M.\} and Chan, \{W. H.\} and T. Mo",

note = "Funding Information: Financial support from the Research Grant Council (HKBC 109/93E) is gratefully acknowledged. ",

year = "1997",

month = apr,

day = "28",

doi = "10.1016/S0040-4039(97)00519-4",

language = "English",

volume = "38",

pages = "3001--3004",

journal = "Tetrahedron Letters",

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TY - JOUR

T1 - Chiral acetylenic sulfoxide in enantioselective synthesis of yohimbine alkaloid

AU - Lee, Albert W.M.

AU - Chan, W. H.

AU - Mo, T.

N1 - Funding Information: Financial support from the Research Grant Council (HKBC 109/93E) is gratefully acknowledged.

PY - 1997/4/28

Y1 - 1997/4/28

N2 - Through Michael addition/acid induced cyclization of secondary amine to chiral acetylenic sulfoxide followed by Pummerer cyclization, an approach to the enantioselective syntheses of pentacyclic yohimbine alkaloids is presented.

AB - Through Michael addition/acid induced cyclization of secondary amine to chiral acetylenic sulfoxide followed by Pummerer cyclization, an approach to the enantioselective syntheses of pentacyclic yohimbine alkaloids is presented.

UR - https://www.scopus.com/pages/publications/0030890687

U2 - 10.1016/S0040-4039(97)00519-4

DO - 10.1016/S0040-4039(97)00519-4

M3 - Journal article

AN - SCOPUS:0030890687

SN - 0040-4039

VL - 38

SP - 3001

EP - 3004

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 17

ER -

Chiral acetylenic sulfoxide in enantioselective synthesis of yohimbine alkaloid

Abstract

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